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rs397516813

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516813(C;C)
Make rs397516813(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12599717
GeneRAF1
is asnp
is mentioned by
dbSNPrs397516813
ebirs397516813
HLIrs397516813
Exacrs397516813
Varsomers397516813
Maprs397516813
PheGenIrs397516813
hapmaprs397516813
1000 genomesrs397516813
hgdprs397516813
ensemblrs397516813
gopubmedrs397516813
geneviewrs397516813
scholarrs397516813
googlers397516813
pharmgkbrs397516813
gwascentralrs397516813
openSNPrs397516813
23andMers397516813
23andMe allrs397516813
SNP Nexus

SNPshotrs397516813
SNPdbers397516813
MSV3drs397516813
GWAS Ctlgrs397516813
Max Magnitude0
ClinVar
Risk rs397516813(C;C)
Alt rs397516813(C;C)
Reference rs397516813(G;G)
Significance Pathogenic
Disease Noonan syndrome not provided
Variation info
Gene RAF1
CLNDBN Noonan syndrome not provided
Reversed 1
HGVS NC_000003.11:g.12641216C>G
CLNSRC
CLNACC RCV000037671.3, RCV000159081.1,